Canonical Allele Identifier: CA344044600

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197404012A>G (hg19) ; chr1:g.197434882A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434882A>G , CM000663.2:g.197434882A>G	GRCh38
NC_000001.10:g.197404012A>G , CM000663.1:g.197404012A>G	GRCh37
NC_000001.9:g.195670635A>G	NCBI36
NG_008483.1:g.171605A>G
NG_008483.2:g.238421A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3019A>G MANE Select	ENSP00000356370.3:p.Arg1007Gly
ENST00000638467.1:c.3019A>G	ENSP00000491102.1:p.Arg1007Gly
ENST00000681519.1:c.1900A>G	ENSP00000505267.1:p.Arg634Gly
ENST00000367397.1:c.1162A>G	ENSP00000356367.1:p.Arg388Gly
ENST00000367399.6:c.2683A>G	ENSP00000356369.2:p.Arg895Gly
ENST00000367400.7:c.3019A>G	ENSP00000356370.3:p.Arg1007Gly
ENST00000484075.5:c.3019A>G	ENSP00000433932.1:p.Arg1007Gly
ENST00000535699.5:c.2947A>G	ENSP00000438786.1:p.Arg983Gly
ENST00000538660.5:c.2129-718A>G	ENSP00000438091.1:n.2129-718A>G
NM_001193640.1:c.2683A>G	NP_001180569.1:p.Arg895Gly
NM_001257965.1:c.2947A>G	NP_001244894.1:p.Arg983Gly
NM_001257966.1:c.2129-718A>G	NP_001244895.1:n.2129-718A>G
NM_201253.2:c.3019A>G	NP_957705.1:p.Arg1007Gly
NR_047563.1:n.3020A>G
NR_047564.1:n.3228A>G
XM_011509365.1:c.3019A>G	XP_011507667.1:p.Arg1007Gly
XM_011509366.1:c.3019A>G	XP_011507668.1:p.Arg1007Gly
XM_011509367.1:c.3019A>G	XP_011507669.1:p.Arg1007Gly
XM_011509368.1:c.2437A>G	XP_011507670.1:p.Arg813Gly
XM_011509369.1:c.1462A>G	XP_011507671.1:p.Arg488Gly
XM_011509365.2:c.3019A>G	XP_011507667.1:p.Arg1007Gly
XM_011509369.2:c.1462A>G	XP_011507671.1:p.Arg488Gly
XM_017000851.1:c.2176A>G	XP_016856340.1:p.Arg726Gly
XM_017000852.1:c.3154A>G	XP_016856341.1:p.Arg1052Gly
NM_201253.3:c.3019A>G MANE Select	NP_957705.1:p.Arg1007Gly
NM_001193640.2:c.2683A>G	NP_001180569.1:p.Arg895Gly
NM_001257965.2:c.2947A>G	NP_001244894.1:p.Arg983Gly
NR_047563.2:n.2972A>G
NR_047564.2:n.3180A>G
NM_001257966.2:c.2129-718A>G	NP_001244895.1:n.2129-718A>G